TIDL CLINICAL CRYOTHERAPY MENTHOL CREAM- clinical cryotherapy menthol cream cream

TIDL CLINICAL CRYOTHERAPY MENTHOL Cream by

Drug Labeling and Warnings

TIDL CLINICAL CRYOTHERAPY MENTHOL Cream by is a Otc medication manufactured, distributed, or labeled by Shenzhen Sam Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Menthol 5%

Purpose

Topical Anesthetic

Use

Temporary relief from minor aches and pains of muscles and joints associated with arthritis simple backache strains and sprains

Warnings

For external use only

Do not use

·do not apply to wounds or damaged skin
·do not apply to irritated skin
·do not bandage
·do not use with heating pad or device

When Using

·avoid contact with the eyes or mucous membranes
·do not apply to wounds or damaged skin
·do not apply to irritated skin
·do not bandage
·wash hands after use with cool water
·do not use with heating pad or device

Stop Use

if condition worsens, or if symptoms persist for more than 7 days or clear up and reoccur again within a few days

Ask Doctor

if condition worsens, or if symptoms persist for more than 7 days or clear up and reoccur again within a few days

Keep Out Of Reach Of Children

If accidentally ingested get medical help or contact a Poison Control Center immediately.

Directions

·Adults and children 12 years of age and older：Apply to affected area not more than 3 to 4 times daily
·Children under 12 years of age：Consult physician

Inactive ingredients

Aminomethyl Propanol, Beta-Caryophyllene（Clove），Carbomer，Caprylyl Glycol，Ceteareth 20 ，
Clove Bud，Disodium EDTA ，Ethyloxiglycerin，Eucalyptus Oil，Glyceryl Stearate，Isopropyl Myristate，
Organic Aloe Vera Juice，Organic Azulene，Propylene Glycol USP，Purified Water，Phenoxyethanol，
Wintergreen Oil

Questions

Call 1（888）778-2986

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TIDL CLINICAL CRYOTHERAPY MENTHOL CREAM 
clinical cryotherapy menthol cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84214-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	5 g  in 0.1 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CAMPHOR OIL (UNII: 75IZZ8Y727)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
CARYOPHYLLENE (UNII: BHW853AU9H)
EUCALYPTUS OIL (UNII: 2R04ONI662)
CETEARETH-20 (UNII: YRC528SWUY)
GAULTHERIA PROCUMBENS (WINTERGREEN) LEAF OIL (UNII: LAV5U5022Y)
ETHYLOXIRANE (UNII: FR67H5388O)
AZULENE (UNII: 82R6M9MGLP)
CARBOMER (UNII: 0A5MM307FC)
AMINOMETHYL PROPANOL (UNII: LU49E6626Q)
CLOVE OIL (UNII: 578389D6D0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84214-010-01	3.785 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/05/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	09/05/2025

Labeler - Shenzhen Sam Technology Co., Ltd. (418511877)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Sam Technology Co., Ltd.		418511877	manufacture(84214-010)